Mutation

Primary Site >> Stomach Cancer

Gene >> NSD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177283893:177283893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6116G>A
AA Mutation	p.Arg2039His(p.R2039H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177251847:177251847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764613088
CDS Mutation	c.4759C>T
AA Mutation	p.Arg1587Cys(p.R1587C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177294548:177294548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7180A>G
AA Mutation	p.Ile2394Val(p.I2394V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177292125:177292125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761103348
CDS Mutation	c.6430G>A
AA Mutation	p.Ala2144Thr(p.A2144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177209751:177209751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1352G>T
AA Mutation	p.Ser451Ile(p.S451I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177292012:177292012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751405024
CDS Mutation	c.6317A>T
AA Mutation	p.Lys2106Met(p.K2106M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177209804:177209804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405G>T
AA Mutation	p.Asp469Tyr(p.D469Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177244258:177244258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4366G>T
AA Mutation	p.Asp1456Tyr(p.D1456Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177238442:177238442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4127C>A
AA Mutation	p.Pro1376His(p.P1376H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177248278:177248278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4595A>T
AA Mutation	p.Gln1532Leu(p.Q1532L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177210875:177210875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2476A>G
AA Mutation	p.Ser826Gly(p.S826G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177294759:177294759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587784216
CDS Mutation	c.7391G>A
AA Mutation	p.Arg2464His(p.R2464H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177260027:177260027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5005C>T
AA Mutation	p.His1669Tyr(p.H1669Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177294435:177294435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780750393
CDS Mutation	c.7067C>T
AA Mutation	p.Thr2356Met(p.T2356M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177210131:177210131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732G>T
AA Mutation	p.Ala578Ser(p.A578S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177267685:177267685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5270G>T
AA Mutation	p.Arg1757Met(p.R1757M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177211106:177211106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2707C>A
AA Mutation	p.Pro903Thr(p.P903T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177211326:177211326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2927C>A
AA Mutation	p.Ala976Asp(p.A976D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177294918:177294918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7550G>A
AA Mutation	p.Gly2517Glu(p.G2517E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177280796:177280796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5854C>T
AA Mutation	p.Arg1952Trp(p.R1952W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177295003:177295003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7635G>T
AA Mutation	p.Lys2545Asn(p.K2545N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177211164:177211164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753460351
CDS Mutation	c.2765C>T
AA Mutation	p.Thr922Met(p.T922M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177211554:177211554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3155G>A
AA Mutation	p.Arg1052His(p.R1052H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000439151
Start	177211997:177211997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367995675
CDS Mutation	c.3598C>T
AA Mutation	p.Arg1200Trp(p.R1200W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439151
Start	177238251:177238251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3936T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439151
Start	177211978:177211978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3579T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439151
Start	177135871:177135871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202191268
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439151
Start	177267614:177267614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779563229
CDS Mutation	c.5199C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439151
Start	177246787:177246787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4488A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439151
Start	177294712:177294712(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7349delA
AA Mutation	p.Asn2450IlefsTer6(p.N2450Ifs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439151
Start	177246749:177246749(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4455delA
AA Mutation	p.Val1486Ter(p.V1486*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439151
Start	177248268:177248268(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4591delA
AA Mutation	p.Met1531CysfsTer43(p.M1531Cfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439151
Start	177273714:177273714(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5556delA
AA Mutation	p.Glu1853SerfsTer2(p.E1853Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439151
Start	177269801:177269801(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5508delA
AA Mutation	p.Ala1837LeufsTer12(p.A1837Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript